La maladie de Parkinson au Canada (serveur d'exploration)

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Death‐associated protein kinase 1 variation and Parkinson’s disease

Identifieur interne : 001868 ( Main/Exploration ); précédent : 001867; suivant : 001869

Death‐associated protein kinase 1 variation and Parkinson’s disease

Auteurs : J. C. Dachsel [États-Unis] ; C. Wider [États-Unis, Suisse] ; C. Vilari O-Güell [États-Unis] ; J. O. Aasly [Norvège] ; A. Rajput [Canada] ; A. H. Rajput [Canada] ; T. Lynch [Irlande (pays)] ; D. Craig [Royaume-Uni] ; A. Krygowska-Wajs [Pologne] ; B. Jasinska-Myga [États-Unis] ; G. Opala ; M. Barcikowska [Pologne] ; K. Czyzewski [Pologne] ; R. Wu [Taïwan] ; M. G. Heckman [États-Unis] ; R. J. Uitti [États-Unis] ; Z. K. Wszolek [États-Unis] ; M. J. Farrer [États-Unis] ; O. A. Ross [États-Unis]

Source :

RBID : ISTEX:AEB952A90DF78BB669F503544B5B54691E9BBCA4

English descriptors

Abstract

Background and purpose:  Mutations of the LRRK2 gene are now recognized as major risk factors for Parkinson’s disease. The Lrrk2 protein is a member of the ROCO family, which also includes Lrrk1 and Dapk1. Functional genetic variants of the DAPK1 gene (rs4877365 and rs4878104) have been previously associated with Alzheimer’s disease.

Url:
DOI: 10.1111/j.1468-1331.2010.03255.x


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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